Canonical Allele Identifier:
CA1140064289
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161493708G= , CM000663.2:g.161493708G= | GRCh38 |
| NC_000001.10:g.161463498G= , CM000663.1:g.161463498G= | GRCh37 |
| NC_000001.9:g.159730122G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922214.1:n.2011+89G= | ||
| XR_922214.2:n.2960+89G= |